|
Symbol Name ID |
Galt
galactose-1-phosphate uridyl transferase MGI:95638 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the nervous system |
Ataxia |
Incoordination |
Clumsiness |
Speech apraxia |
Action tremor |
Postural tremor |
Abnormality of mental function |
Delayed speech and language development |
Dysarthria |
Deficit in grammar |
Speech articulation difficulties |
Depression |
Anxiety |
Lethargy |
Autistic behavior |
Attention deficit hyperactivity disorder |
Mental deterioration |
Intellectual disability |
Intellectual disability, mild |
Dystonia |
Gait disturbance |
Gait imbalance |
Encephalopathy |
Global developmental delay |
Specific learning disability |
Seizure |
| Disease(s) Associated with GALT | |||||||||||||||||||||||||||
| classic galactosemia |
| Mouse Phenotypes | cerebral edema |
brain inflammation |
abnormal cerebellum external granule cell layer morphology |
abnormal Purkinje cell morphology |
decreased Purkinje cell size |
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| Availability | Mouse Genotype | |||||
| GaltGt(E285B04)Wrst/GaltGt(E285B04)Wrst | ||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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